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1 a potential tool to reduce the incidence of congenital toxoplasmosis.
2 we developed a novel chicken embryo model of congenital toxoplasmosis.
3 Approximately fifteen million of these have congenital toxoplasmosis.
4 s of clinical symptoms and disability due to congenital toxoplasmosis.
5 ancy was not associated with a lower rate of congenital toxoplasmosis.
6 after infection was fully effective against congenital toxoplasmosis.
7 ng pregnancy, and 1.0 per 10 000 infants had congenital toxoplasmosis (13% mean transmission rate).
8 toxoplasmosis, 1 sample from a patient with congenital toxoplasmosis, 22 samples from soldiers opera
10 manifestations were observed in infants with congenital toxoplasmosis after a waterborne toxoplasmosi
11 e summarize current prevention strategies of congenital toxoplasmosis and evaluate options to improve
12 rasite burden is associated with severity of congenital toxoplasmosis and indicate that serological t
13 m 1987 to 2008 and assessed how the risks of congenital toxoplasmosis and of clinical signs at age 3
14 reliosis, cat scratch disease, toxocariasis, congenital toxoplasmosis, and invasive aspergillosis.
15 e to listeriosis was lower than those due to congenital toxoplasmosis but accords with those due to e
16 developed to derive estimates of the risk of congenital toxoplasmosis by exact duration of gestation
18 remarkable finding in infants with treated, congenital toxoplasmosis, consonant with their improved
21 otozoan parasite Toxoplasma gondii can cause congenital toxoplasmosis (CT), an often fatal or lifelon
24 tional infections with Toxoplasma gondii and congenital toxoplasmosis in Austria, a country with a na
27 icant reduction in risk of clinical signs of congenital toxoplasmosis in infected children born from
29 rain: We identified susceptibility genes for congenital toxoplasmosis in our cohort of infected human
31 imester was associated with a higher rate of congenital toxoplasmosis independent of maternal treatme
32 of grade 2 NCMD, and in this single family, congenital toxoplasmosis is a phenocopy of grade 3 NCMD.
39 ublic health primarily within the context of congenital toxoplasmosis or postnatally acquired disease
40 12 gene has susceptibility alleles for human congenital toxoplasmosis (rs6502997 [P, <0.000309], rs31
41 in the National Collaborative Chicago-Based Congenital Toxoplasmosis Study (NCCCTS) have a high inci
44 nochoroidal lesion formation in infants with congenital toxoplasmosis that may be relevant in the est
47 this study, susceptibility alleles for human congenital toxoplasmosis were identified in the NALP1 ge
48 phy was performed in 56 infants with treated congenital toxoplasmosis when they were newborns and app